P
US9546226B2ActiveUtilityPatentIndex 51

Catalyst for living radical polymerization and polymerization method

Assignee: GOTO ATSUSHIPriority: Aug 6, 2009Filed: May 10, 2010Granted: Jan 17, 2017
Est. expiryAug 6, 2029(~3.1 yrs left)· nominal 20-yr term from priority
Inventors:GOTO ATSUSHITSUJII YOSHINOBUFUKUDA TAKESHI
C08F 12/08C08F 2438/00C08F 293/005C08F 120/14C08F 4/40
51
PatentIndex Score
1
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30
References
10
Claims

Abstract

Provided is a low-cost, highly active, environmentally friendly living radical polymerization catalyst which does not require a radical initiator. An organic compound having an oxidation-reduction capability is used as a catalyst. Even if a radical initiator is not used, a monomer can be subjected to a radical polymerization to obtain a polymer having narrow molecular weight distribution. The cost of the living radical polymerization can be remarkably reduced. It is made possible to prevent adverse effects of using a radical initiator. The present invention is significantly more environmentally friendly and economically excellent than conventional living radical polymerization methods, due to advantages of the catalyst such as low toxicity of the catalyst, low amount of the catalyst necessary, high solubility of the catalyst, mild reaction conditions, and no coloration/no odor (which do not require a post-treatment for a molded article), etc.

Claims

exact text as granted — not AI-modified
The invention claimed is: 
     
       1. A method of polymerization comprising:
 polymerizing, in a living radical polymerization, a monomer of the formula CH 2 ═CR 5 R 6 , hydrogen or a C 1-3  alkyl group and R 6  is a carbon/late, C 1-10  aryl or a C 6-10  aromatic group, by contacting the monomer with an organic halide and an organic compound 
 wherein: 
 the organic halide is of the formula CR 2 R 3 R 4 X 3 , wherein R 2  and R 3  are each independently hydrogen or C 1-10 , R 4  is halogen, hydrogen, C 1-10  alkyl, a C 6-10  aromatic group, a C 5-10  heteroaryl group containing at least one heteroatom or cyano, and X 3  is halogen, and
 the organic compound is selected from the group consisting of: 
 
 triethylamine; 
 tributylamine; 
 tetrakis(dimethylamino) amine; 
 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane; 
 Tributylphosphine; 
 N,N,N′,N″,N″-pentamethyl diethylenetriamine; 
 ethylenediamine; 
 dimethyl ethylenediamine; 
 tetramethylethylenediamine; 
 tetramethyldiaminomethane; 
 tris(2-aminoethyl)amine; 
 tris(2-(methylamino)ethyl)amine; 
 1,2-bis(diphenylphosphino)methane; 
 hematoporphyrin; 
 triethylphosphine; 
 triphenylphosphine; 
 phosphonic acid; 
 1,2-bis(diphenylphosphino)methane; 
 thiophene; 
 oligothiophene; 
 polythiophene; 
 tetrathiofulvalene; 
 bis(ethylenedithio)tetrathiafulvalene; 
 3,4-ethylenedioxythiophene; and 
 poly(3,4-ethylenedioxythiophene); 
 the living radical polymerization is conducted without the use of a catalyst other than the organic compound, 
 a raw material composition which is used in the method does not include a raw material containing a transition metal, and 
 a radical initiator is not added to a reaction mixture at the time of conducting the living radical polymerization. 
 
     
     
       2. The method of  claim 1 , wherein R 6  is a carboxylate or a C 6  aromatic group. 
     
     
       3. The method of  claim 2 , wherein R 6  is carboxylate, phenyl or naphthyl. 
     
     
       4. The method of  claim 1 , wherein R 2  is and R 3  are each independently hydrogen or C 1-5  alkyl. 
     
     
       5. The method of  claim 1 , wherein R 4  is halogen, hydrogen, C 1-5  alkyl, a C 6-10  aromatic group, a C 5-10  heteroaryl group containing at least one heteroatom or cyano. 
     
     
       6. The method of  claim 1 , wherein R 4  is a C 6-10  aromatic group,
 a C 5-10  heteroaryl group containing at least one heteroatom or cyano. 
 
     
     
       7. The method of  claim 5 , wherein R 4  is a C 6-10  aromatic group,
 a C 5-10  heteroaryl group containing at least one heteroatom or cyano. 
 
     
     
       8. The method of  claim 1 , wherein R 5  is hydrogen or a C 1-3  alkyl group and R 6  is a carboxylate or a C 6  aromatic group. 
     
     
       9. The method of  claim 1 , wherein the monomer is selected from the group consisting of (meth)acrylic acid ester; a styrene monomer; (meth)acrylonitrile; (meth)acrylamide; a vinyl ester monomer; (meth)acrylic acid; and vinyl halide. 
     
     
       10. The method of  claim 1 , wherein the organic compound is selected from the group consisting of:
 triethylamine; 
 tributylamine; 
 tetrakisdimethylaminoethene; 
 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane; 
 tributylphosphine; 
 triphenylphosphine; 
 bis(ethylenedithio)tetrathiafulvalene; 
 ethylenediamine; 
 dimethylethylenediamine; 
 tetramethylethylenediamine; 
 tetramethyldiaminomethane; 
 tris(2-aminoethyl)amine; 
 tris(2-(methylamino)ethyl)amine; 
 1,2-bis(diphenylphosphino)methane; and 
 hematoporphyrin.

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